4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

Base Information

Chemical Name:4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine
CAS No.:1266156-94-8
Molecular Formula:C₂₄H₁₈N₄O
Molecular Weight:378.433
Hs Code.:

Synonyms:4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

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Chemical Property of 4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

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Technology Process of 4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

There total 6 articles about 4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1266161-23-2
2-chloro-3-fluoro-5-(4-phenoxyphenyl)isonicotnonitrile

: 98-80-6
phenylboronic acid

: 1266156-94-8
4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

Guidance literature:: With potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; In 1,4-dioxane; at 100 ℃; for 4h; Inert atmosphere; Sealed tube;

Reference yield:

: 153463-65-1
3,5-dichloropyridine-4-carbonitrile

: 1266156-94-8
4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium phosphate / palladium diacetate; 1,1'-bis(di-tertbutylphosphino)ferrocene / 1,4-dioxane / 20 h / Inert atmosphere; Sealed tube; Reflux

2.1: potassium fluoride / dimethyl sulfoxide / 240 h / 120 °C

3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 18 h / 20 °C

4.1: trichlorophosphate / 1.5 h / 100 °C

4.2: 0 °C

5.1: potassium phosphate / palladium diacetate; 1,1'-bis(di-tertbutylphosphino)ferrocene / 1,4-dioxane / 4 h / 100 °C / Inert atmosphere; Sealed tube

With potassium fluoride; potassium phosphate; 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; In 1,4-dioxane; dichloromethane; dimethyl sulfoxide; 5.1: Suzuki Coupling;

Reference yield:

: 1266161-17-4
3-chloro-5-(4-phenoxyphenyl)isonicotinonilrile

: 1266156-94-8
4-(4-phenoxyphenyl)-7-phenyl-1H-pyrazolo[3,4-c]pyridin-3-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium fluoride / dimethyl sulfoxide / 240 h / 120 °C

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 18 h / 20 °C

3.1: trichlorophosphate / 1.5 h / 100 °C

3.2: 0 °C

4.1: potassium phosphate / palladium diacetate; 1,1'-bis(di-tertbutylphosphino)ferrocene / 1,4-dioxane / 4 h / 100 °C / Inert atmosphere; Sealed tube

With potassium fluoride; potassium phosphate; 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; In 1,4-dioxane; dichloromethane; dimethyl sulfoxide; 4.1: Suzuki Coupling;